A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540341



Internal ID20913631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156380107..156380694hg38UCSC Ensembl
chr1:156349898..156350485hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247742
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540341
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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